一只患有高醛固酮症的猫在肾上腺切除术后出现了持久的低醛固酮症。

IF 0.7 Q3 VETERINARY SCIENCES
Journal of Feline Medicine and Surgery Open Reports Pub Date : 2024-05-12 eCollection Date: 2024-01-01 DOI:10.1177/20551169241243012
Léa Bouccara, Antoine Dunie-Merigot, Laure Poujol, Laurent Blond, Franck Jolivet
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引用次数: 0

摘要

病例摘要:一只 10 岁的绝育雄性短毛猫因腹部肿块、伴有肾衰竭、慢性呕吐、厌食和持续 3 周的进行性多尿/多脂症而就诊。临床检查和初步血检显示该猫患有氮质血症、低钾血症和高血压。腹部超声波检查显示,右肾附近有一个直径 3 厘米的肾上腺肿块。高血清醛固酮提示原发性高醛固酮症。手术发现了肿块,并将其与右肾上腺一并切除。组织学诊断为肾上腺皮质癌。术后,血清肌酐和血钾升高,血清醛固酮偏低,诊断为低醛固酮症。患者需要接受为期 6 个月的矿物皮质激素治疗,结果临床和生物学状况均有所改善:据我们所知,本病例描述了在单侧肾上腺切除术治疗肾上腺癌并伴有高醛固酮症后,猫继发性低醛固酮症的最长持续时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-lasting hypoaldosteronism after adrenalectomy in a cat with hyperaldosteronism.

Case summary: A 10-year-old neutered male domestic shorthair cat was presented with an abdominal mass, associated renal failure, chronic vomiting, anorexia and progressive polyuria/polydipsia lasting for 3 weeks. Clinical examination and initial blood work revealed azotaemia, hypokalaemia and hypertension. Abdominal ultrasound showed an adrenal mass with a diameter of 3 cm near the right kidney. High serum aldosterone suggested primary hyperaldosteronism. Surgery enabled identification of the mass and its excision along with the right adrenal gland. Histologically, carcinoma of the adrenal cortex was diagnosed. Postoperatively, an increase in serum creatinine and potassium, along with a low serum aldosterone, led to a diagnosis of hypoaldosteronism. Mineralocorticoid therapy for 6 months was necessary, resulting in clinical and biological improvement.

Relevance and novel information: To our knowledge, this case describes the longest-lasting reported secondary hypoaldosteronism in a cat, after unilateral adrenalectomy for an adrenal carcinoma with hyperaldosteronism.

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来源期刊
CiteScore
1.30
自引率
14.30%
发文量
57
审稿时长
15 weeks
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